Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1317589749
rs1317589749
FGB
2 0.925 0.080 4 154570471 missense variant T/A snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs75848804
rs75848804
FGG
4 0.882 0.080 4 154604995 missense variant G/A;C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs772014512
rs772014512
FGB
2 0.925 0.080 4 154567772 missense variant C/T snv 4.8E-05 1.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs894077860
rs894077860
FGB
2 0.925 0.080 4 154569660 stop gained C/T snv 0.010 1.000 1 2013 2013